Establishment registration
Yiwu Ori-Power Medtech Co., Ltd.
FDA establishment registration 3012309743 · YIWU Zhejiang, CN
Key facts
| Registration number | 3012309743 |
|---|---|
| Establishment name | Yiwu Ori-Power Medtech Co., Ltd. |
| Owner/operator | Yiwu Ori-Power Medtech Co.,Ltd. |
| Owner/operator number | 10051297 |
| FEI number | 3012309743 |
| Address | No.86 Xiahe Road, Beiyuan Street, Yiwu, |
| City | YIWU Zhejiang |
| Country | CN |
| Establishment types | Contract manufacturer |
| Registration valid through | 2026 |
| Product codes listed | BTQ, BYG, BYP, CCX, EFN, FLL, FMA, FQM, FRL, FSM, FXX, GAX, GFC, HMP, HSP, HTD, HXQ, IAL, ILH, ILI, IMD, IQI, IQK, IWP, JCE, JOK, KGX, KME, KMJ, KOZ and 16 more |
| Device classes | 1, 2, N, U |
At a glance
- 10–99 Device listings
- 10–99 UDI devices (GUDID)
- Current Registration current
- None FDA inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device establishment registrations
Device establishments that manufacture, repackage, relabel or import devices for the U.S. market must register annually with the FDA and list the devices they produce.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database